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The authors thank Zsolt Karanyi 1st Department of Internal Medicine, MHSCUD ; for the statistical analysis and the staff of the HPOG in the study. This work was supported by the grant of the Health Science Council of the Ministry of Health, Republic of Hungary ETT ; No. 225. 149; you may develop a headache because of this medicine, but do not stop taking it. Background-Reductions in basal limb blood flow have been implicated in the pathogenesis of metabolic syndrome and functional impairment in humans. We tested the hypothesis that reductions in limb blood flow and vascular conductance with age are either absent or attenuated in those who perform regular strength training. Methods-A total of 104 apparently healthy normotensive men aged 20-35 young ; and 35-65 years middle-aged ; who were either sedentary or resistance trained were studied. Results-Systolic, mean, and diastolic blood pressures were higher P 0.05-0.001 ; in the middle-aged compared with the young men, but there were no significant differences between the sedentary and resistance-trained groups. In sedentary group, basal femoral blood flow duplex Doppler ultrasound ; and vascular conductance were lower P 0.001 ; in the middle-aged compared with the young men. There were no such age-related differences in resistance-trained group. In the young men, femoral blood flow and vascular conductance were not different between the two activity groups, but, in the middle-aged men, they were ~27% higher P 0.01 ; in the resistance-trained men than in the sedentary men. These activity related differences in limb blood flow was associated with ~15% higher leg fat-free mass DEXA; P 0.01 ; in the resistance-trained men than their sedentary peers r 0.37-0.43, P 0.001 ; . Conclusions-We concluded that the age-related reductions in basal whole-limb blood flow and vascular conductance are absent in resistance-trained men. These results suggest that resistance training may favorably influence leg perfusion in aging humans through its impact on leg skeletal muscle mass. Content provided by cerner multum, inc what is the most important information i should know about fosinopril and hydrochlorothiazide. Ational Institutes of Health NIH ; consensus and stateof-the-science statements are prepared by independent panels of health professionals and public representatives on the basis of 1 ; the results of a systematic literature review prepared under contract with the Agency for Healthcare Research and Quality AHRQ ; , 2 ; presentations by investigators working in areas relevant to the conference questions during a 2-day public session, 3 ; questions and statements from conference attendees during open discussion periods that are part of the public session, and 4 ; closed deliberations by the panel during the remainder of the second day and the morning of the third. This statement is an independent report of the panel and is not a policy statement of the NIH or the federal government. The statement reflects the panel's assessment of medical knowledge available at the time the statement was written. Thus, it provides a "snapshot in time" of the state of knowledge on the conference topic. When reading the statement, keep in mind that new knowledge is inevitably accumulating through medical research. Menopause is a natural process that occurs in women's lives as part of normal aging. Many women go through the menopausal transition with few or no symptoms, while some have significant or even disabling symptoms. Menopause is defined by the World Health Organization and the Stages of Reproductive Aging Workshop STRAW ; working group as the permanent cessation of menstrual periods that occurs naturally or is induced by surgery, chemotherapy, or radiation. Natural menopause is recognized after 12 consecutive months without menstrual periods that are not associated with a physiologic e.g., lactation ; or pathologic cause. Menopausal transition often begins with variations in length of the menstrual cycle. The hormonal changes during the menopausal transition can span several years. The following 3 periods or intervals were defined by experts at the STRAW working group in 2001: 1. Reproductive stage: From menarche first menstrual period ; to the beginning of the perimenopause when cycles become variable ; . 2. Menopausal transition: The time of an increase in follicle-stimulating hormone and increased variability in cycle length, 2 skipped menstrual cycles with 60 or more days of amenorrhea absence of menstruation ; , or both. The menopausal transition concludes with the final menstrual period FMP ; and the beginning of postmenopause.

During 19931994, all computerized general practices in Oxfordshire were invited to take part in a post-marketing surveillance study of proton pump inhibitors.3 Forty-two 58 per cent ; practices agreed to take part. These practices identified 1102 patients who had been prescribed proton pump inhibitors. Eight hundred and ninety-two 81 per cent ; patients gave written consent to be included in the study. These patients were sent a postal questionnaire with up to two reminders, which included questions about current and past use of alcohol and tobacco. The questions were the same as had been used in a previous survey of healthy lifestyles carried out in the Oxford region see Table 1 ; .4 Two years later, during 19951996, the GP records of these patients were reviewed, and information including alcohol and tobacco use was abstracted. A research nurse looked at both the computer record and the most recent recording of lifestyle in the patients' case notes. If the computer record disagreed with the case note, then whichever had been amended most recently was used. If patients were recorded as `non-smokers' as opposed to ex-smokers or never smokers, then the research nurse looked back in the record for any previous and hydrocodone.
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337 LEFT VENTRICULAR MASS INDEX AND 48-HOURS BLOOD PRESSURE MONITORING IN HEMODIALYSIS PATIENTS R. Ekart, R. Hojs, V. Kanic, S. Bevc, B. Dvorsak, B. Balon-Pecovnik Maribor, Slovenia ; 338 EFFECT OF CALCIUM SUPPLEMENTATION ON PREVENTION OF PREGNANCY INDUCED HYPERTENSION IN IRAN M. Kashanian, M. Rayka Tehran, Iran ; 339 CALCIUM MOBILIZATION, PHOSPHATIDYLSERINE AND MICROPARTICLES IN PLATELETS OF HYPERTENSIVES MEASURED BY FLOW CYTOMETRY. EFFECT OF DOXAZOSIN GITS M. Labis, M. Martnez, F. Gabriel, V. Guiral, S. Ruiz-Aja, M.A. Hernndez-Presa * , J. Aznar Valencia, * Madrid, Spain ; 340 EFFECTS OF DIFFERENT CLASSES OF ANTIHYPERTENSIVE AGENTS ON PULSE PRESSURE M. Anghel, M. Macri, V. Greere, E. Radu Sultanescu, A. Gutu Bucharest, Romania ; 341 BLOOD PRESSURE NORMALIZATION WITH AMLODIPINE IN PREVIOUSLY UNCONTROLLED HYPERTENSIVE PATIENTS IN GENERAL PRACTICE IN BELGIUM P. Van der Niepen, K. Houbracken Brussels, Belgium ; 342 IS DOPAMINE A MODULATOR OF CARDIOVASCULAR RESPONSE IN HYPERTENSIVE SUBJECTS? F. Contreras, J. Rocafull, M. Carrucci, J. Cevallos, C. Fouillioux, G. Ibez, M. Gonzlez, M. Velasco, G.A. Cabezas Caracas, Venezuela ; 343 HEART RATE VARIABILITY AND ECG CHANGES IN 148 DANISH PATIENTS AFTER TWO YEARS IN THE VALUE TRIAL O.L. Pedersen, J. Refsgaard, E.S. Nielsen Viborg, Denmark ; 344 THE ROLE OF AMLODIPINE IN A GLOBAL CV RISK MANAGEMENT PROGRAM IN POSTMENOPAUSAL HYPERTENSIVE WOMEN P. van der Niepen, C. Brohet, K. Houbracken Brussels, Belgium ; 345 DIFFERENCES IN LEFT ATRIAL SYSTOLIC FUNCTION IN PRIMARY AND FAMILIAL AMYLOIDOSIS I. Moyssakis, D. Papadopoulos, E. Gialafos, A. Zilidis, V. Votteas, F. Triposkiadis Athens, Greece ; 346 FIXED-DOSE VALSARTAN + HYDROCHLOROTHIAZIDE COMBINATION THERAPY COMPARED WITH AMLODIPINE MONOTHERAPY IN HYPERTENSIVE PATIENTS WITH ADDITIONAL CARDIOVASCULAR RISK FACTORS: THE VAST STUDY L. Ruilope, E. Malacco * , Y. Khder * , G. Brnner * , D. Heintz * Madrid, Spain; * Milan, Italy; * Basel, Switzerland; * Bad Krozingen, Germany ; 347 24-HOUR AMBULATORY BLOOD-PRESSURE EFFECTS OF VALSARTAN + HYDROCHLOROTHIAZIDE COMBINATIONS COMPARED WITH AMLODIPINE IN HYPERTENSIVE PATIENTS AT INCREASED CARDIOVASCULAR RISK L. Ruilope, D. Heintz * , A. Brandao * , P. Stolt * , A. Kandra * , M. Santonastaso * , Y. Khder * Madrid, Spain; * Basel, Switzerland; * Sao Paolo, Brazil; * Vittorio Veneto-TV, Italy ; 348 DO BULGARIAN GENERAL PRACTITIONERS KNOW THE DEFINED TARGET LEVELS FOR BLOOD PRESSURE CONTROL - RESULTS FROM BULPRAKT-HEARTSTUDY B. Georgiev, N. Gotcheva, V. Baytcheva, D. Gotchev Sofia, Bulgaria.

LOUISIANA MEDICAID PROGRAM ISSUE DATE: 12 01 05 PROVIDER MANUAL REVISED DATE: CHAPTER 37: PHARMACY BENEFITS MANAGEMENT SERVICES SECTION: 37.16 PATIENT COUNSELING, DRUG UTILIZATION REVIEW DUR ; AND PROVIDER PEER BASED PROFILING and ibuprofen.

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WEB TABLE Randomised placebo-controlled trials testing five categories of blood pressure lowering drugs in fixed dose - numbers of participants and treatment arms testing each drug, present standard daily dose of each drug, and cost to the British National Health Service of one year's supply at standard doses Total number of participants Standard daily Cost of one year Drug treatment arms ; in trials dose mg ; supply British ; Thiazides Hydrochlorothiazidew1-34 2458 56 ; 25 5 Chlorthalidonew35-46 908 18 ; 25 11 Indapamidew47-55 668 11 ; 2.5 37 Bendroflumethiazidew56-60 285 9 ; 2.5 10 Metolazonew61 78 3 ; 2 Chlorothiazidew38, w62 64 4 ; 250 * Cyclopenthiazidew63 41 3 ; 0.25 17 Beta-blockers B1 selective Atenololw14, w39, w43, w60, w64-88 1276 38 ; 50 9 Bisoprololw17, w25, w29, w89-93 950 15 ; 10 125 Betaxololw94-96 601 6 ; 20 98 Metoprololw36, w43, w75, w77, w87, w97-104 547 16 ; 100 22 Celiprololw105, 106 70 3 ; 200 222 Acebutololw60, 107 43 3 ; 400 261 Non-selective Nebivololw71, 108-110 619 10 ; 5 128 Pindololw11, w51, w60, w77, w86, w104, w111-114 384 12 ; 15 87 Propranololw13, w60, w80, w84, w98, w101, w115-119 339 15 ; 160 12 Bopindololw120 86 3 ; 1 * Oxprenololw84, w87, 73 3 ; 80 37 Timololw12, w60 50 3 ; 10 Nadololw121, w122 33 2 ; 80 blocking action 70 4 ; 25 164 Carvedilolw123, w124 Labetalolw58, w60 48 3 ; 400 84 ACE inhibitors Enalaprilw10, w13, w65, w66, w76, w125-150 1682 49 ; 10 68 Perindoprilw5, w150-157 1054 21 ; 4 159 Captoprilw6, w7, w86, w158-167 1048 22 ; 50 38 Trandolaprilw168-177 1001 18 ; 1 135 Cilazaprilw23, w178-186 871 23 ; 2.5 107 Ramiprilw4, w187-193 737 18 ; 2.5 98 Lisinoprilw34, w137, w194-202 651 14 ; 10 126 Quinaprilw20, w203-207 625 15 ; 20 117 619 ; 10 157 Fosinoprilw16, w21, w208-210 Spiraprilw3, w211-w214 583 13 ; 6 * Benazeprilw18, w26, w215, w216 334 7 ; 20 * 145 3 ; 15 122 Moexiprilw15, w217 Angiotensin-II receptor antagonists Candesartanw144, w218-w228 2894 33 ; 8 195 2880 ; 80 205 Valsartanw19, w139, w158, w195, w229-232 Losartanw9, w140-142, w224, w225, w229, w233-240 2296 24 ; 50 225 Olmesartanw241 2243 6 ; 20 * 1143 19 ; 150 214 Irbesartanw30, 233, w242-246 Telmisartanw234, w247, w248 661 14 ; 40 164 Tasosartanw249-252 417 7 ; 50 * Eprosartanw253-255 306 4 ; 600 192 Calcium-channel blockers Dihydropyridines 1335 37 ; 5 106 Felodipinew135, w150, w193, w256-272 Isradipinew273-287 1151 30 ; 5 178 Nifedipinew31, w37, w42, w83, w88, w167, w268, w288-303 1082 31 ; 40 105 631 ; 5 154 Amlodipinew215, w216, w288, w304-310 Nicardipinew311-318 358 11 ; 90 175 Lercandipinew319 161 3 ; 10 127 148 ; 20 171 Nisoldipinew320 Lacidipinew8, w79, w321-324 145 7 ; 4 199 Nitrendipinew70, 149 71 2 ; 20 * Non-dihydropyridines w 1668 33 ; 240 77 Diltiazem 2, w24, w28, w74, w136, w194, w199, w325-w333 Verapamilw43, w65, w116, w117, w138, w170, w171, w173, w177, w305, w334-343 1248 35 ; 240 27 Should be taken more than once daily in divided doses, or a sustained release preparation used * Not marketed in Britain. Other health problems, and the Centers for Disease Control and Prevention recommends that people over age 65 get a single dose of the pneumococcal vaccine. You should also have a tetanus shot every 10 years. Continue to practice safe sex. See your dentist once or twice a year. After age 40, reading may may need to hold things farther away in order to see them clearly. Perhaps you need reading glasses. Your eye doctor may also want to check for glaucoma, which becomes more common after your forties. It can damage your vision before you realize you have it. Take your medicines as instructed, and be sure every doctor that you see knows all the drugs you are currently taking. This includes over-thecounter ones such as vitamins, dietary supplements, painkillers, and antihistamines. Some drug stores even keep a computer file of all your prescriptions so that they can check for dangerous drug interactions if a new medicine is added. Stay active--both physically and mentally. If you don't work outside of the home, consider getting a part-time job or volunteer with a nonprofit organization. Find a hobby. Learn to and imitrex.
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Tell your health care provider if you are taking any other medicines, especially any of the following: anticoagulants eg, warfarin ; because side effects, including risk of bleeding, may be increased by acarbose calcium channel blockers eg, verapamil ; , corticosteroids eg, prednisone ; , diuretics eg, hydrochlorothiazide ; , estrogen, isoniazid, nicotinic acid, oral contraceptives birth control pills ; , phenothiazines eg, chlorpromazine ; , phenytoin, sympathomimetics eg, pseudoephedrine ; , or thyroid hormone because the effectiveness of acarbose may be increased or decreased insulin or sulfonylureas eg, glyburide ; because side effects may be increased by acarbose digoxin because its effectiveness may be decreased by acarbose this may not be a complete list of all interactions that may occur and isosorbide.
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A. DIURETICS Generic Name Acetazolamide Amiloride Bendroflumethiazide Benzthiazide Bumetanide Chlorothiazide Cyclothiazide Ethacrynic Acid Flumethiazide Furosemide Hydrochlorothiazide Hydroflumethiazide Methyclothiazide Metolazone Polythiazide Probenecid Quinethazone Spironolactone Triamterene Trichlormethiazide and related substances B. EPITESTOSTERONE C. PROBENECID Brand Names Examples ; Amilco Midamor Aprinox Aquatag Burine Diuril Anhydron Edecrin --Lasix Aprozide Leodrine Aquatensen Zaroxolyn Renese Benemid Hydromox Aldactone Jatropur, Dytac Anatran and lanoxin. No drug interactions of clinical significance have been identified for candesartan cilexetil. Compounds which have been investigated in clinical pharmacokinetic studies include hydrochlorothiazide, warfarin, digoxin, oral contraceptives i.e. ethinylestradiol levonorgestrel ; , glibenclamide and nifedipine. The bioavailability of candesartan is not affected by food. The antihypertensive effect of Blopress Comp may be enhanced by other antihypertensives. The potassium depleting effect of hydrochlorothiazide could be expected to be potentiated by other drugs associated with potassium loss and hypokalaemia e.g. other kaliuretic diuretics, laxatives, amphotericin, carbenoxolone, penicillin G sodium, salicylic acid derivates.

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Medications for ovulation induction other medications for women medications for men medications for ovulation induction the many medicines used to treat female infertility fall into two groups: drugs used to promote ovulation, and drugs used to treat other hormonal problems associated with infertility and lescol. The smc has also accepted losartan hydrochlorothaizide cozaar-comp 100 25 from merck, sharp & dohme ; for use within nhs scotland for the treatment of essential hypertension in patients whose blood pressure is not adequately controlled on hydrochlorothiazide or losartan monotherapy.

Glucomed 625 mg tablets 2. QUALITATIVE AND QUANTITATIVE COMPOSITION and levaquin and hydrochlorothiazide. Zestoretic lisinopril and hydrochlorothiazide ; in patients with severe congestive heart failure, with or without associated renal insufficiency, excessive hypotension has been observed and may be associated with oliguria and or progressive azotemia, and rarely with acute renal failure and or death. In many of the decisions in which a differential diagnosis has been deemed reliable, the party relying on the diagnosis has offered independently reliable evidence that the allegedly dangerous drug or substance had harmful effects and levothroid. TO THE EDITOR : I wish to report hyponatraemia in a patient commencing therapy with mirtazapine -- this is the first such report from Australia. An 86-year-old widow with depression had had a previous episode of hyponatraemia while taking venlafaxine. Anticipating the possibility of further hyponatraemia, I prescribed mirtazapine 15 mg nightly -- half the recommended starting dose. At this time, she was also taking amiodarone, gliclazide, L -thyroxine, irbesartan with hydrochlorothiazide, alendronate, omeprazole, atorvastatin and zolpidem. Her baseline serum sodium level was 135 mmol L normal range [NR], 135 149 mmol L ; , but 4 days later it had.

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Formation of a more slowly excreted, active metabolite.10 Currently, losartan is indicated for hypertension, although it may be useful in congestive heart failure as well.11 In clinical trials the effect of losartan emerges slowly. In one such trial extended-release felodipine reduced blood pressure to a greater extent than losartan at 6 weeks, but by 12 weeks there was no difference in response.12 Adding small doses of hydrochlorothiazide to losartan increases the antihypertensive efficacy of the latter drug.13 In many studies hydrochlorothiazide was added at 4 to weeks for patients not responding to losartan alone.13, 14 It is arguable that the full effect of losartan monotherapy takes longer to occur and that adding a second drug before 12 weeks is unnecessary. In the only published comparison of losartan and amlodipine, patients who did not respond to losartan were given hydrochlorothiazide after only 4 weeks.14 We therefore designed a study to compare the effects, over 12 weeks, of losartan alone, losartan with hydrochlorothiazide, and amlodipine in patients with mild or moderate essential hypertension. In addition to the standard measurement of blood pressure, we performed ambulatory blood pressure monitoring ABPM ; in one-third of the patients. In ABPM a portable, automatic device is used to obtain and store blood pressure readings at predetermined times throughout a given period, usually 24 hours. The development of ABPM has provided an accurate means to as. Drug HYDROCODONE W APAP ZITHROMAX FUROSEMIDE NORVASC LIPITOR SINGULAIR POTASSIUM CHLORIDE PLAVIX TOPROL XL IBUPROFEN ZYRTEC RANITIDINE HCL AMOXICILLIN PROPOXYPHENE NAP. W APAP PROMETHAZINE HCL LOTREL ZOLOFT CEPHALEXIN GABAPENTIN ALBUTEROL HYDROCHLOROTHIAZIDE OMNICEF LEXAPRO AMOX TR-POTASSIUM CLAVULANATE SEROQUEL TOTAL TOP 25 Total Rx Claims From 01 05-01 Health Information Designs, Inc. 3 it is time to recognize that 25 mg of hydrochlorothiazide is inadequate for many african american patients with resistant hypertension, and in many cases, represents undertreatment and hydrocodone.
Hydrochlorothiazide use in free access to lisinopril and depressed mood or information on the drug lisinopril altering in patients with a study of concomitant administration of the risk of snake venom. Pharmacotherapy , 24 1 ; : 799 credits kathleen ariss, ms christopher wood, md, facs - urology oncology author: reviewed by: martin gabica, md - family medicine , christopher wood, md, facs - urology oncology editors: kathleen ariss, ms, terrina vail 1995-2007, healthwise, incorporated. Labetalol lacticare hydrocortisone . lactulose . 24, 25 LAMICTAL . LAMISIL . 26, 33 lamotrigine . LANOXICAPS . LANOXIN . LANTUS . LARIAM . 26, 33 LASIX . leena . leflunomide . LESCOL . 13, 37 LESCOL XL 13, 37 lessina . leucovorin calcium . LEUKERAN . leuprolide LEVAQUIN . 28, 33 LEVATOL . LEVEMIR . LEVITRA . LEVLEN . LEVLITE . levobunolol . levora levorphanol . levothroid . levothyroxine . levoxyl . LEVULAN KERA . LEXAPRO . 17, 39, 41 LEXIVA . LEXXEL . lidazone . lidocaine . lidocaine hydrocortisone . 20, 25 lidocaine prilocaine . LIDODERM . lindane LIPEX . LIPITOR . 13, 37, 41 lipram . lipram CR lipram PN lipram UL lisinopril . 10, 35 lisinopril hydrochlorothiazide . 11 lithium carbonate lithium carbonate CR lithium citrate . LITHOBID . OVRAL. Propoxyphene hcl .T-4 propoxyphene hcl acetaminophen .T-4 propoxyphene acetaminophen .T-4 propranolol hcl .T-29 propranolol hydrochlorothiazid .T-30 propylthiouracil .T-57 PROQUAD .T-59 Proscar.T-44 Prosed Ec .T-58 PROSED DS .T-58 Prostigmin .T-47 PROSTIGMIN .T-47 PROTONIX .T-26 PROTONIX IV .T-26 Proventil.T-57 PROVENTIL HFA .T-57 PROVIGIL.T-5 Prozac.T-49 pseudoephed tan dexchlor tan .T-39 pseudoephedrine hcl .T-56 Psorcon E .T-19 Psoriatec.T-42 P-Tex.T-39 PULMICORT .T-1 Purinethol.T-23 pv w-o cal ferrous fumarate fa.T-46 pv w-o vit a iron, carbonyl fa.T-46 pyrazinamide.T-21 Pyridium.T-25 pyridostigmine bromide .T-47 Questran .T-20 Questran Light .T-20 QUICK MIX W LYTES.T-32 Quinaglute.T-33 quinapril hcl.T-52 quinapril hydrochlorothiazide .T-52 Quinidex.T-33 quinidine gluconate.T-33 QUINIDINE GLUCONATE .T-33 quinidine sulfate.T-33 QVAR .T-1 RABAVERT .T-59 RANEXA.T-33 ranitidine hcl.T-26 RAPAMUNE .T-45 RAPTIVA .T-55. Studies reporting on short-term crisis containment i.e., the use of drug treatments to achieve rapidonset management of suicidality in individuals in psychiatric emergencies. Genotypic resistance: the genetic code of hiv has mutations that are linked to drug resistance.

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HOW DOES THE PREOPERATIVE EVALUATION OF POTENTIAL SPK RECIPIENTS DIFFER FROM THAT OF KIDNEY TRANSPLANT ALONE KTA ; RECIPIENTS? At Harper University Hospital, the preoperative evaluation of the potential SPK recipient does not differ substantially from that of the diabetic KTA recipient. Heart catheterization is performed in virtually all patients. If significant and correctable blockages are detected in the coronary arteries, candidates should undergo balloon angioplasty or bypass surgery prior to transplantation. An ultrasound of the gallbladder is obtained in all patients. If gallstones are present, the gallbladder must be removed prior to transplantation. IS YOUR OWN PANCREAS REMOVED WHEN WE PERFORM THE TRANSPLANT? No. We do not even come close to the area where your own pancreas is located during the transplant operation. HOW DOES THE SPK PROCEDURE DIFFER FROM KTA? In KTA, the kidney is placed outside the abdominal cavity through an incision made along the groin area, usually on the right side. The artery and vein of the kidney transplant are attached to the groin artery and vein, and the ureter is attached to the bladder. The procedure usually takes 4-6 hours. In SPK, the organs are placed within the abdominal cavity through an incision going down the middle of the abdomen. If you are on peritoneal dialysis and have a catheter in your abdomen, it is removed at the time of transplant. The pancreas is attached to the groin vessels on the right side of your pelvis and the kidney is attached to the groin vessels on the left side of your pelvis. The duodenum of the pancreas transplant is connected to your small intestine and the ureter of the kidney transplant is connected to your bladder. The procedure usually takes 5-7 hours see diagram on page 4 ; . HOW LONG WILL I BE IN THE HOSPITAL AFTER THE TRANSPLANT? You can expect to be in the hospital for 5-7 days after the transplant. If you have complications, your stay could be longer. HOW DOES THE POSTOPERATIVE CARE OF THE SPK PATIENT DIFFER FROM THAT OF THE KTA PATIENT? Since the SPK procedure is performed in, rather than outside, the abdominal cavity, your bowels will not function well immediately after the surgery. For this reason, a nasogastric so-called NG ; tube is inserted through your nose down into your stomach while you are asleep on the operating table, and will need to be left in place to decompress your bowels until they begin to function, usually on the third or fourth day after transplant. You will.




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